QA Vacancies At Elixir Pharma

📌We Are Hiring: Compliance Specialist!

Elixir Pharma is looking for a highly skilled Compliance Specialist to join our QA team

📍 Work location: EL Sadat City – EL Menoufia.

◼️Key Responsibilities:

• Ensure compliance with GMP, regulatory guidelines, and internal company policies.

• Monitor and review company processes to ensure adherence to compliance standards.

• Support preparation for regulatory inspections and internal audits.

• Participate in deviation, CAPA, and change control processes.

• Review and maintain compliance documentation, SOPs, and policies.

• Conduct compliance risk assessments and recommend corrective actions when required.

• Collaborate with QA, QC, Regulatory Affairs, and other departments to ensure regulatory alignment.

• Support training programs related to compliance and regulatory requirements.

• Ensure proper documentation practices and maintain data integrity standards.

• Contribute to continuous improvement initiatives to strengthen the compliance framework.

◼️What we are looking for in the ideal candidate

• Bachelor’s degree in Pharmacy, Science, or a related field.

• 1-3 years of experience in Compliance, QA, or Regulatory Affairs within a pharmaceutical company.

• Strong knowledge of GMP, regulatory guidelines, and pharmaceutical quality systems.

• Excellent documentation and analytical skills.

• Strong attention to detail and problem-solving abilities

◼️Ready to join and make a real impact:

Interested candidates should send their CV to hr@elixirpharma-eg.com

Subject Line: Compliance Specialist.

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We Are Hiring: IPC Supervisor!

Elixir Pharma is looking for a highly skilled IPC Supervisor to join our QA team

📍 Work location: EL Sadat City – EL Menoufia.
◼️Key Responsibilities:
• Supervise in-process control (IPC) activities during manufacturing operations.
• Ensure that all production stages comply with cGMP requirements and quality standards.
• Monitor critical process parameters and ensure compliance with approved specifications.
• Review IPC test results and ensure timely reporting and documentation.
• Coordinate closely with Production, QA, and QC departments to resolve any process deviations.
• Investigate out-of-specification (OOS) or abnormal results and support root cause analysis.
• Ensure proper sampling and testing during manufacturing processes.
• Review batch records related to IPC activities.
• Train and guide IPC team members on procedures, GMP practices, and safety requirements.
• Participate in continuous improvement initiatives to enhance process efficiency and product quality.